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Merck
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重要文件

N2915

Sigma-Aldrich

PYR-41

≥98% (HPLC), powder

同義詞:

4-[4-[(5-硝基-2-呋喃基)亚甲基]-3,5-二氧代-1-吡唑烷基]苯甲酸乙酯

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About This Item

經驗公式(希爾表示法):
C17H13N3O7
CAS號碼:
分子量::
371.30
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

品質等級

化驗

≥98% (HPLC)

形狀

powder

顏色

red to brown

溶解度

DMSO: 5 mg/mL, clear (warmed)

儲存溫度

−20°C

SMILES 字串

CCOC(=O)c1ccc(cc1)N2NC(=O)\C(=C/c3ccc(o3)[N+]([O-])=O)C2=O

InChI

1S/C17H13N3O7/c1-2-26-17(23)10-3-5-11(6-4-10)19-16(22)13(15(21)18-19)9-12-7-8-14(27-12)20(24)25/h3-9H,2H2,1H3,(H,18,21)/b13-9+

InChI 密鑰

ARGIPZKQJGFSGQ-UKTHLTGXSA-N

應用

PYR-41已被用作E1抑制剂:
  • 用于确定腺相关病毒(AAV)转导的细胞降解途径
  • 通过基质辅助激光解吸/电离飞行时间(MALDI-TOF)E2/E3分析,评估其选择性和效力
  • 处理高葡萄糖培养基中完全分化的C2C12肌管,以确定其对蛋白质泛素化和细胞活力的影响
  • 预处理人脑微血管内皮细胞(hBMEC),用于细菌感染前的抑制研究

生化/生理作用

PYR-41是泛素活化酶(E1)的细胞渗透性抑制剂.
PYR-41是泛素活化酶(E1)的细胞渗透性抑制剂,对E3、E2或半胱天冬酶的活性几乎无活性或完全无活性。
PYR-41能够抑制E1泛素连接酶,如小鼠双微基因2同源物(MDM2)、痒同源物(ITCH)和HOIL-1L相互作用蛋白(HOIP)的E1泛素连接酶。 它具有潜在的抗癌作用。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral - Skin Sens. 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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